CA2868156A1 - Composes de pyridopyrimidine substituee et leur utilisation comme inhibiteurs de flt3 - Google Patents

Composes de pyridopyrimidine substituee et leur utilisation comme inhibiteurs de flt3 Download PDF

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Publication number
CA2868156A1
CA2868156A1 CA2868156A CA2868156A CA2868156A1 CA 2868156 A1 CA2868156 A1 CA 2868156A1 CA 2868156 A CA2868156 A CA 2868156A CA 2868156 A CA2868156 A CA 2868156A CA 2868156 A1 CA2868156 A1 CA 2868156A1
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CA
Canada
Prior art keywords
compound
administration
amino
leukemia
pharmaceutically acceptable
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CA2868156A
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English (en)
Other versions
CA2868156C (fr
Inventor
Hong Woo Kim
Hee Kyu Lee
Ho-Juhn Song
Jaekyoo Lee
Jong Sung Koh
Jung-Ho Kim
Se Won Kim
In Yong Lee
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Oscotec Inc
Original Assignee
Oscotec Inc
Genosco
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Publication date
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Publication of CA2868156A1 publication Critical patent/CA2868156A1/fr
Application granted granted Critical
Publication of CA2868156C publication Critical patent/CA2868156C/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/28—Compounds containing heavy metals
    • A61K31/305—Mercury compounds
    • A61K31/31—Mercury compounds containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Transplantation (AREA)
  • Oncology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
CA2868156A 2012-03-22 2013-03-15 Composes de pyridopyrimidine substituee et leur utilisation comme inhibiteurs de flt3 Active CA2868156C (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261614274P 2012-03-22 2012-03-22
US61/614,274 2012-03-22
PCT/US2013/032575 WO2013142382A1 (fr) 2012-03-22 2013-03-15 Composés de pyridopyrimidine substituée et leur utilisation comme inhibiteurs de flt3

Publications (2)

Publication Number Publication Date
CA2868156A1 true CA2868156A1 (fr) 2013-09-26
CA2868156C CA2868156C (fr) 2020-07-28

Family

ID=49223277

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2868156A Active CA2868156C (fr) 2012-03-22 2013-03-15 Composes de pyridopyrimidine substituee et leur utilisation comme inhibiteurs de flt3

Country Status (22)

Country Link
US (1) US8877763B2 (fr)
EP (1) EP2828259B1 (fr)
JP (1) JP6101341B2 (fr)
KR (1) KR102011770B1 (fr)
CN (1) CN104428298B (fr)
AU (1) AU2013235344B2 (fr)
BR (1) BR112014023460B1 (fr)
CA (1) CA2868156C (fr)
CL (1) CL2014002505A1 (fr)
EA (1) EA031267B1 (fr)
ES (1) ES2694223T3 (fr)
HK (1) HK1208453A1 (fr)
IL (1) IL234802B (fr)
IN (1) IN2014MN02082A (fr)
MX (1) MX360912B (fr)
MY (1) MY184858A (fr)
NZ (1) NZ700283A (fr)
PL (1) PL2828259T3 (fr)
SG (1) SG11201405942RA (fr)
TR (1) TR201816480T4 (fr)
WO (1) WO2013142382A1 (fr)
ZA (1) ZA201407588B (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102228034B1 (ko) * 2013-10-21 2021-03-16 제노스코 치환된 피리미딘 화합물 및 syk 억제제로서의 이의 용도
CN105272930B (zh) * 2014-07-17 2018-07-13 广东东阳光药业有限公司 取代脲衍生物及其在药物中的应用
KR20160035411A (ko) * 2014-09-23 2016-03-31 주식회사 오스코텍 LRRK2 (Leucine Rich Repeat Kinase 2) 키나제 억제제로서의 피리도피리미딘 유도체 화합물
EP3220914B1 (fr) 2014-11-17 2020-09-02 Rhode Island Hospital Compositions de nanomatériau, synthèse et assemblage
US20210275532A1 (en) * 2018-06-27 2021-09-09 Oscote Inc. Pyridopyrimidinone derivatives for use as axl inhibitors
KR20200022712A (ko) * 2018-08-23 2020-03-04 주식회사 오스코텍 8-브로모-2-(1-메틸피페리딘-4-일아미노)-4-(4-페녹시페닐아미노)피리도[4,3-d]피리미딘-5(6H)-온 염산염의 결정다형체 및 그 제조방법
KR102230721B1 (ko) * 2019-02-01 2021-03-22 주식회사 오스코텍 피리도피리미딘계 염산염을 포함하는 경구용 고형제제 및 이의 제조방법
US20220143049A1 (en) 2019-03-21 2022-05-12 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
CN110327347B (zh) * 2019-08-16 2021-06-01 陕西科技大学 G-749在制备抗真菌药物中的应用
TWI759829B (zh) * 2019-08-23 2022-04-01 財團法人生物技術開發中心 作為第iii型受體酪胺酸激酶抑制劑之雜環吡唑衍生物
EP4054579A1 (fr) 2019-11-08 2022-09-14 Institut National de la Santé et de la Recherche Médicale (INSERM) Méthodes pour le traitement de cancers qui ont acquis une résistance aux inhibiteurs de kinase
WO2021148581A1 (fr) 2020-01-22 2021-07-29 Onxeo Nouvelle molécule dbait et son utilisation
WO2023027966A1 (fr) 2021-08-24 2023-03-02 Biomea Fusion, Inc. Composés de pyrazine en tant qu'inhibiteurs irréversibles de flt3
TW202340177A (zh) 2021-12-30 2023-10-16 美商拜歐米富士恩股份有限公司 作為 flt3抑制劑之吡嗪化合物
WO2023225005A1 (fr) 2022-05-17 2023-11-23 Biomea Fusion, Inc. Polythérapie à base de flt3 pour le cancer et compositions associées
KR102440707B1 (ko) 2022-07-10 2022-09-05 이우미 공장 추천 시스템

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2394525A1 (fr) * 2000-01-27 2001-08-02 Warner-Lambert Company Derives de pyridopyrimidinone destines au traitement de maladies maladie neurodegenerative
WO2002018379A2 (fr) * 2000-08-31 2002-03-07 F. Hoffmann-La Roche Ag 7-oxo pyridopyrimidines
CA2420286A1 (fr) * 2000-08-31 2002-03-07 F. Hoffmann-La Roche Ag 7 oxo pyridopyrimidines comme inhibiteurs d'une proliferation cellulaire
EP2025678A1 (fr) * 2007-08-17 2009-02-18 Oncalis AG Composés pyrazolo[3,4-d]pyrimidine et leur utilisation comme modulateur de protein kinase
TW200942537A (en) * 2008-02-01 2009-10-16 Irm Llc Compounds and compositions as kinase inhibitors
EP2330909B1 (fr) * 2008-08-12 2013-09-18 GlaxoSmithKline LLC Composés chimiques
US8338481B2 (en) * 2009-01-28 2012-12-25 Ramot At Tel-Aviv University Ltd. Alkoxyalkyl S-prenylthiosalicylates for treatment of cancer
EP2467137A1 (fr) * 2009-08-19 2012-06-27 Ambit Biosciences Corporation Composés biaryles et procédés d utilisation de ceux-ci
TR201802464T4 (tr) * 2009-10-29 2018-03-21 Genosco Ki̇naz i̇nhi̇bi̇törleri̇

Also Published As

Publication number Publication date
CL2014002505A1 (es) 2015-10-02
NZ700283A (en) 2016-08-26
MX2014011354A (es) 2014-12-05
AU2013235344B2 (en) 2017-03-16
KR102011770B1 (ko) 2019-08-19
US20130274274A1 (en) 2013-10-17
PL2828259T3 (pl) 2019-02-28
MX360912B (es) 2018-11-22
EP2828259A4 (fr) 2015-08-19
EA201491747A1 (ru) 2015-10-30
ES2694223T3 (es) 2018-12-19
IL234802B (en) 2018-10-31
KR20140144709A (ko) 2014-12-19
CN104428298B (zh) 2017-03-01
TR201816480T4 (tr) 2018-11-21
CN104428298A (zh) 2015-03-18
SG11201405942RA (en) 2014-10-30
BR112014023460B1 (pt) 2020-09-01
JP6101341B2 (ja) 2017-03-22
EA031267B1 (ru) 2018-12-28
EP2828259B1 (fr) 2018-08-08
MY184858A (en) 2021-04-27
US8877763B2 (en) 2014-11-04
ZA201407588B (en) 2015-11-25
AU2013235344A1 (en) 2014-10-09
EP2828259A1 (fr) 2015-01-28
HK1208453A1 (en) 2016-03-04
CA2868156C (fr) 2020-07-28
JP2015510942A (ja) 2015-04-13
IN2014MN02082A (fr) 2015-08-21
WO2013142382A1 (fr) 2013-09-26

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Effective date: 20171212